Hemostasis valve for guide catheter control

ABSTRACT

An extension member is has a body with a proximal end and an opposing distal end. It includes a hollow lumen extending therethrough from the proximal end to the distal end. It has a female luer lock connector proximate its proximal end and a male luer lock connector proximate its distal end. Its body has an outer surface with a driven member.

CROSS-REFERENCE TO RELATED PATENT APPLICATIONS

This application is a continuation of U.S. application Ser. No.15/252,561, filed Aug. 31, 2016, entitled “HEMOSTASIS VALVE FOR GUIDECATHETER CONTROL” which is a continuation of U.S. application Ser. No.14/020,487, filed Sep. 6, 2013, entitled “HEMOSTASIS VALVE FOR GUIDECATHETER CONTROL”, which claims the benefit of U.S. ProvisionalApplication No. 61/832,227, filed Jun. 7, 2013, entitled “GUIDE CATHETERDRIVE”, and U.S. Provisional Application No. 61/699,711, filed Sep. 11,2012, entitled “HEMOSTASIS VALVE AND SYSTEM FOR GUIDE CATHETER CONTROL”and U.S. Provisional Application No. 61/697,734, filed Sep. 6, 2012,entitled “HEMOSTASIS VALVE FOR GUIDE CATHETER CONTROL”, all of which areincorporated herein by reference in their entireties.

BACKGROUND

The present invention relates generally to the field of catheter systemsfor performing diagnostic and/or intervention procedures. The presentinvention relates specifically to a hemostasis valve for guide cathetercontrol in robotic catheter system.

Vascular disease, and in particular cardiovascular disease, may betreated in a variety of ways. Surgery, such as cardiac bypass surgery,is one method for treating cardiovascular disease. However, undercertain circumstances, vascular disease may be treated with a catheterbased intervention procedure, such as angioplasty. Catheter basedintervention procedures are generally considered less invasive thansurgery.

During one type of intervention procedure, a guide catheter is insertedinto a patient's femoral artery and positioned proximate the coronaryostium of a patient's heart. A guide wire is inserted into the guidecatheter typically through a hemostasis valve and maneuvered through thepatient's arterial system until the guide wire reaches the site of thelesion. A working catheter is then moved along the guide wire until theworking catheter such as a balloon and stent are positioned proximatethe lesion to open a blockage to allow for an increased flow of bloodproximate the lesion. In addition to cardiovascular disease, otherdiseases may be treated with catheterization procedures.

SUMMARY OF THE INVENTION

In one embodiment a hemostasis valve is provided which has a valve bodywith a first and second leg. The first leg has a proximal port, a distalport and a lumen extending between the proximal port and the distalport. At least one valve is located in the lumen adjacent the proximalport to permit an interventional device to be passed therethrough. Thesecond leg extends at an angle relative to the first leg and is in fluidcommunication with the first leg. A rotating male luer lock connector isrotatably connected to the first leg proximate to the distal port and isconfigured to secure a guide catheter thereto. The rotating male luerlock connector has a driven member configured to be rotatably driven bya drive mechanism. The rotating male luer lock connector is rotatinglycoupled with the guide catheter.

In another embodiment a combined hemostasis valve and extension memberis provided. The hemostasis valve has a valve body with a first andsecond leg. The first leg has a proximal port, a distal port and a lumenextending between the proximal port and the distal port. At least onevalve is located in the lumen adjacent the proximal port to permit aninterventional device to be passed therethrough. The second leg extendsat an angle relative to the first leg and is in fluid communication withthe first leg. A rotating male luer lock connector is rotatablyconnected to the first leg proximate to the distal port. The extensionmember has a proximal end coupled to the rotating male luer lockconnector and a distal end configured to secure a guide catheterthereto. It also has a driven member configured to be rotatably drivenby a drive mechanism.

In a further embodiment an extension member is additionally providedthat has a body with a proximal end and an opposing distal end. Itincludes a hollow lumen extending therethrough from the proximal end tothe distal end. It has a female luer lock connector proximate itsproximal end and a male luer lock connector proximate its distal end.Its body has an outer surface with a driven member.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is an isometric view of a hemostasis valve.

FIG. 2 is a schematic view of a robotic catheter control system.

FIG. 3 is an isometric view of a catheter bedside system.

FIG. 4 is an isometric view of a catheter bedside system.

FIG. 5 is an isometric view of a hemostasis valve and guide catheterdrive mechanism

FIG. 6 is a cross-sectional view a hemostasis valve.

FIG. 7 is a top view of the catheter bedside system of FIG. 2.

FIG. 8 is a side view of the catheter bedside system of FIG. 2.

FIG. 9 is an isometric view of the guide catheter drive mechanism andtrack.

FIG. 10 is a cross sectional view of the track.

FIG. 11 is a top schematic view of the hemostasis valve, guide wire,working catheter, and guide catheter.

FIG. 12 is a rear isometric view of the catheter bedside system.

FIG. 13 is an alternative hemostasis valve and guide catheter drivemechanism.

FIG. 14 is a partial side view of the hemostasis valve and guidecatheter.

FIG. 15 is a partial side view of an alternative guide catheter hub andguide catheter drive mechanism.

FIG. 16 is an isometric view of a quick release for a hemostasis valve.

FIG. 17 is a cross sectional view of a portion of the quick release ofFIG. 16. in an engaged position.

FIG. 18 is a cross sectional view of a portion of the quick release ofFIG. 16. in a disengaged position.

FIG. 19 is an isometric view of an extension member rotatably coupling amale rotating luer lock of a hemostasis valve which is affixed to thebase which carries a drive member.

FIG. 20 is an exploded view of the guide catheter, extension member andhemostasis valve of FIG. 19.

FIG. 21 is a cross-sectional view of FIG. 19 taken generally along line21-21.

FIG. 22 is another embodiment of a friction drive member driving anouter surface of a rotating male luer lock of the hemostasis valve.

DETAILED DESCRIPTION OF THE EXAMPLE EMBODIMENTS

Referring to FIG. 1, a Y-connector or hemostasis valve 34 includes avalve body with a first leg 38 having a proximal port adjacent aproximal end 42 and a distal port adjacent a distal end 40. First leg 38includes lumen extending between the proximal end 42 and the distal end40. A valve 162 is disposed adjacent proximal end 42. A rotating luerconnector 48 is rotatably secured to first leg 38 proximate distal end40. Rotating luer connector 48 includes a member 56 configured to berotatably driven by a drive mechanism of a robotic catheter system 10.

Referring to FIG. 2, a robotic catheter system 10 includes a bedsidesystem 12, a work station 14 including a controller 16, a user interface18 and display 20. Bedside system 12 is located adjacent a patient bed22 and an imaging system 24. Imaging system 24 may be any medicalimaging system that may be used in conjunction with a catheter basedmedical procedure (e.g., non-digital x-ray, digital x-ray, CT, MRI,ultrasound, etc.).

In one embodiment, imaging system 24 is a digital x-ray imaging devicethat is in communication with workstation 14. Imaging system 24 isconfigured to take x-ray images of the appropriate area of patientduring a particular procedure. For example, imaging system 24 may beconfigured to take one or more x-ray images of the heart to diagnose aheart condition. Imaging system 24 may also be configured to take one ormore x-ray images during a catheter based medical procedure (e.g.,real-time images) to assist the user of workstation 14 to properlyposition a guide wire, guide catheter, and a working catheter such as astent during a procedure. The image or images may be displayed ondisplay 20 to allow the user to accurately steer a distal tip of a guidewire or working catheter into proper position. As used herein thedirection distal is used to refer to the direction closer to a patientin the intended use of the component and the term proximal is used torefer to the direction further away to a patient in the intended use ofthe component.

Referring to FIG. 3 bedside system 12 includes a guide cathetermechanism 26, a working catheter mechanism 28 and a guide wire mechanism30. In one embodiment, working catheter mechanism 28 and guide wiremechanism 30 are of the type described in U.S. Pat. No. 7,887,549entitled “Catheter System” which is incorporated herein in its entirety.

Referring to FIGS. 3-5 guide catheter mechanism 26 includes a base 32configured to releasably receive a hemostasis valve 34 and a guidecatheter rotational drive 36. Base 32 may include a quick releasemechanism to releasably secure hemostasis valve 34 to base 32. Oneembodiment of a guide catheter quick release is disclosed in USapplication publication US 2012/0179032 entitled “Remote Catheter SystemWith Steerable Catheter” which is incorporated herein in its entirety.

Hemostasis valve 34 includes a first leg 38 having a distal end 40 and aproximal end 42. A second leg 44 extends from first leg 38 and is influid communication with first leg 38 such that a fluid may beintroduced into a proximate end 46 of second leg 44. Hemostasis valvefirst leg 38 defines a longitudinal axis 50 extending from proximal end42 of first leg 38 to distal end 40 of first leg 38.

The distal end 40 of first leg 38 includes a rotating luer connector 48that is rotatably coupled to distal end 40 of first leg 38. Rotatingluer connector 48 includes an external surface 52 and an internal region54 having a luer female interface to releasably couple a guide catheter.Luer connectors are known in the art and provide a fluid tightconnection between a guide catheter and a hemostasis valve. Luerconnectors are covered by standards such as ISO 594 (including sections594-1 and 594-2) and EN 1707.

In one embodiment external surface 52 of rotating luer connector 48includes a driven member such as gear 56 that is driven by drivemechanism including a rotational drive 36. Rotational drive 36 includesa driven member such as a drive gear 58 operatively connected to a motor60. Gear 56 may be integrally formed with rotating luer connector 48 andcoupled with a drive gear 58 for rotational movement of the rotatingconnector. The driven member as described herein may include a beveledgear, a friction surface, or a surface configured to receive a belt andthe drive member may include a beveled gear, a wheel, or a belt.

In another embodiment, gear 56 may be secured to the outer surface ofrotational luer connector 48 such that gear 56 rotates along with therotation of rotational luer connector 48 about longitudinal axis 50 ofthe first leg 38 of hemostasis valve 34.

Gears 56 and 58 may be beveled gears or miter gears to provide directrotation of driven gear 56 from a shaft rotated by motor 60 andextending along an axis 62 perpendicular to longitudinal axis 50 offirst leg 38 of hemostasis valve 34. Motor 60 rotates in a firstdirection 61 about axis 62 of the motor and an opposing second direction63 about axis 62 of the motor. Referring to FIG. 1, gear 56 is beveledsuch that gear teeth 64 extend in a direction toward proximal end 42 andaway from distal end 40 of first leg 38. Additionally, in one embodimentdriven gear 56 is located a distance from distal end 40 to permitattachment and removal of a guide catheter from rotational luerconnector 48. Drive gear 58 is positioned below first leg 38 to permiteasy removal of the hemostasis valve 34 from base 32.

Motor 60 may be secured to base 32, such that drive gear 58 is locatedabove a first surface 66 of base 32 and motor 60 is located below anopposing second surface 68 of base 32. First surface 66 being closer tofirst leg 38 than second surface 68 of base 32.

Referring to FIG. 1 FIG. 6 second leg 44 of hemostasis valve 34 has alongitudinal axis 70 extending longitudinally along second leg 44 fromproximate end 46 to a distal end 72 adjacent first leg 38. A second legworking plane is defined by axis 50 of first leg 38 and axis 70 ofsecond leg 44. In one embodiment hemostasis valve 34 is secured to base32 such that the second leg working plane is not perpendicular to thehorizontal as defined by gravity. Rather the second leg working planeforms an acute angle with respect to a vertical plane permitting anoperator access to proximate end 46 of second leg 44. In one embodimentsecond leg working plane may be co-planer with a horizontal plane. Asdiscussed above, hemostasis valve 34 may be releasably coupled to base32 with a quick release that allows removal of hemostasis valve 34 frombase 32.

Referring to FIG. 5, base 32 includes a raised wall 74 extendingupwardly from and perpendicular to surface 66. Wall 74 extends in adirection parallel to axis 50 of hemostasis valve 34, when hemostasisvalve 34 is secured to base 32. Wall 74 is proximate a rear portion 76of base 32 and distal a front portion 78 of base 32. Gear 58 beingintermediate wall 74 and front portion 78 of base 32. A guide member 80is secured to wall 74 and extends in a direction substantially parallelto axis 50 when hemostasis valve 34 is secured to base 32. Guide member80 has a guide portion 82 configured to direct a portion of a guidecatheter prior to the guide catheter entering a sleeve 84. Referring toFIG. 5 and FIG. 6, a first or distal linear bearing surface 139 isoperatively connected to base 32 The distal linear bearing surface 139contacts a rotatable linear bearing surface 65 prohibiting movement ofthe rotating connector 48 in a proximal direction 51 parallel to a valvebody longitudinal axis colinear with axis 50. A second or proximallinear bearing surface 141 is operatively connected to base 32. Proximallinear bearing surface 141 contacts a linear bearing surface 67 onhemostasis valve 34. First leg 38 of hemostasis valve 34 includes atransition portion 69 to linear bearing surface 67. Referring to FIG. 6transition portion 69 is arcuate. Base 32 contacts linear bearingsurface 67 and does not contact the transition portion 69. Statedanother way proximal linear bearing surface 141 contacts linear bearingsurface 67 and does not contact transition portion 69. Distal linearbearing surface 139 and proximal linear bearing surface 141 interactswith linear bearing surface 65 and linear bearing surface 67respectively to locate hemostasis valve 34 with respect to base 32 andaligns driven member 56 with drive member 58. Distal linear bearingsurface 139 interacts with linear bearing surface 65 to prohibitmovement of hemostasis valve 34 in proximal direction 51 which is thedirection along axis 50 from the distal port toward the proximal port.Proximal linear bearing surface 141 interacts with hemostasis valvelinear bearing surface 67 to prohibit movement of hemostasis valve 34 ina distal direction 53 which is the direction along axis 50 opposite theproximal direction 51. Rotatable linear bearing surface 65 is proximateto and rotates with driven member 56. A longitudinal slot having alongitudinal opening is defined by and extends from the distal linearbearing surface and the proximal linear bearing surface. Referring toFIG. 5 and FIG. 14 hemostasis valve 34 is positioned within longitudinalslot. A finger 145 proximate longitudinal slot prohibits movement of thehemostasis valve in a direction perpendicular to longitudinal axis 50from longitudinal slot through the longitudinal opening.

Referring to FIG. 3 and FIG. 10 a track 86 includes a channel 88. A setscrew 90 or other type of fastener extends through track 86 into channel88 to secure sleeve 84. In one embodiment sleeve 84 includes a firstwall 92 and a second wall 94 and a third wall 96 extending from firstwall 92 forming a cavity 98. An opening 100 is defined as the spacebetween the two free ends of second wall 94 and third wall 96. Inanother embodiment, sleeve 84 may be formed by a single arcuate wallmember having an opening 100. A disposable sterile barrier sleeve suchas a plastic sleeve may be located about track 86 such that when sleeve84 is isolated from track 86. Sleeve 84 may be a single use device anddisposed of once a medical procedure using the sleeve is complete. Inanother embodiment, no sleeve 84 is placed into channel 88, rather asterile barrier may be placed within channel 88 to isolate a guidecatheter from the walls of channel 88. In an alternative embodiment, nosleeve or sterile barrier is employed and track 86 is a single usedevice that is discarded after use and replaced prior to the use of thebedside system with another patient or for another procedure.

Referring to FIG. 7 and FIG. 8 track 86 includes a distal end 102 thatis configured to be located proximate a patient, and an opposingproximal end 104. A track longitudinal axis 106 is defined by thelongitudinal axis of the track 86 extending between proximal end 104 anddistal end 102. In one embodiment track longitudinal axis 106 andhemostasis valve longitudinal axis 50 form an acute angle 108. In oneembodiment angle 108 is preferably between 25 and 45 degrees, and morepreferably between 30 and 45 degrees. In one embodiment angle 108 is 30degrees.

In one embodiment plane track longitudinal axis 106 forms an acute angle112 with a horizontal plane defined by gravity that also represents thehorizontal plane of a bed or procedural surface that a patient lies on.Track longitudinal axis 106 and hemostasis valve first leg longitudinalaxis 50 form a plane 110. In one embodiment plane 110 is at an acuteangle 108 with respect to the horizontal plane. In other embodiments,the angle formed between plane 110 and the horizontal may be an acuteangle different than the angle formed by track longitudinal axis 106 andthe horizontal plane.

Referring to FIGS. 7 and 8 guide catheter mechanism 26 is offset to oneside of track 86, as a result plane 110 is not perpendicular to thehorizontal plane. In one embodiment guide catheter mechanism 26 islocated closer to an operator than track 86. Stated another way, when anoperator operates guide catheter mechanism 26 the operator will becloser to the guide catheter mechanism than the track.

Referring to FIG. 3, in one embodiment, track 86, guide cathetermechanism 26 and cassette 118 may be rotated downwardly about axis ysuch that guide catheter mechanism 26 and cassette 118 are easier toaccess by an operator facing guide catheter mechanism 26 and cassette118. In one embodiment, the vector shown as x is perpendicular to thelongitudinal axis 106 extends through channel 88 and forms an angle 166below a horizontal plane. In one embodiment angle 166 is 15 degreesbelow a horizontal plane as defined by gravity. In one embodiment anoperator is located proximate a first side a patient's bed. A support islocated on one side of the bed typically opposite the first side. Thecassette 118 and guide catheter mechanism 26 is closer to the first sideof the patient's bed than track 86. In this way, the operator orphysician has easy access to the cassette 118 and guide cathetermechanism 26. By tilting the cassette 118 and guide catheter mechanismdownwardly toward the patient's bed such that the portion of thecassette 118 and guide catheter mechanism 26 closer to track 86 ishigher vertically than the portion of the cassette 118 and guidecatheter mechanism 26 that is furthest from track 86. Additionally, bypivoting guide catheter mechanism 26 and cassette 118 from thelongitudinal axis 106 by angle 108, the guide catheter mechanism andcassette 118 is located in a position that allows for access by theoperator and/or physician.

Track 86 is secured to a bedside support 114 and is maintained in afixed position relative to patient bed 22. Bedside support 114 may besecured directly to a side of patient bed 22 or may be secured to afloor mounted support that is either fixed relative patient bed 22 orpositioned on a floor proximate patient bed 22 such that track 86 is ina fixed location with respect to patient bed 22 or to a patient onpatient bed 22 during a catheter based procedure. In one embodiment, theorientation of track 86 may be adjusted with respect to patient bed 22so that angle 112 may be adjusted as well. In another embodiment angle112 may be between ten degrees and forty five degrees and in oneembodiment angle 112 may be thirty degrees.

Referring to FIG. 12 guide catheter mechanism 26 may be secured to alinear actuator 116 to translate guide catheter mechanism along an axisparallel to or co-linear with track axis 106. The linear actuator 116may provide for discrete incremental movement or may provide forcontinuous movement. In one embodiment the linear actuator includes arack and pinion and in another embodiment includes a robotic arm. Linearactuator 116 moves independently of track 86. As discussed above workingcatheter mechanism 28 and guide wire mechanism 30 may be included in acassette 118 that is operatively removably secured to a base member 120.Base member 120 and guide catheter mechanism 26 may be operativelysecured to linear actuator 116 with a support 164, such that guidecatheter mechanism 26, working catheter mechanism 28, and guide wiremechanism 30 are translated together along a linear axis.

The operation of the guide catheter mechanism 26 during a catheterprocedure will now be described using an exemplary embodiment. A patientin need of a catheter based procedure will lie in a supine position onpatient bed 22. An opening in the femoral artery will be prepared forthe introduction of a guide catheter 122.

Track 86 will be positioned relative to the patient such that distal end102 of track 86 is located proximate the femoral artery of the patient.Track 86 is covered with a sterile barrier and a single used sleeve 84is positioned in channel 88. Typically track 86 will be covered with asterile barrier prior to positioning relative to the patient. As sleeve84 is positioned in channel 88 the sterile barrier is placed intochannel 88 such that the sterile barrier provides a guard against anyfluids that may be exposed on sleeve 84 from contacting track 86. Sleeve84 has a distal end 124 and a proximal end 126. Distal end 124 of sleeve84 is located proximal distal end 102 of track 86. In one embodiment,sleeve 84 may have certain geometry to provide for placement withinchannel 88 of track 86 and to facilitate entry and removal of a portionof guide catheter 122.

In one catheter procedure on the heart of a patient, a guide catheter122 of appropriate length is selected based on the size of the patient.Guide catheter 122 has a proximal end 128 and a distal end 130. In oneembodiment, proximal end 128 is first connected to rotating luerconnector 48 of hemostasis valve 34. Distal end 130 is then manuallyinserted into the femoral artery of the patient and positioned such thatdistal end 130 of the guide catheter 122 is located adjacent the ostiumof the heart. It is also contemplated that proximal end 128 of guidecatheter 122 may be connected to rotating luer connector 48 after distalend 130 is positioned adjacent the ostium.

Once guide catheter 122 is properly positioned relative to the patient'sheart, a central portion 132 of guide catheter 122 located outside ofthe patient is placed within sleeve 84 by pushing a central portion 132of guide catheter 122 through opening 100 into cavity 98.

Referring to FIG. 9 and FIG. 11, an entering portion 134 of guidecatheter 122 will be exposed between distal end 102 of track 86 and thepatient. Additionally, a connecting portion 136 adjacent proximal end124 of guide catheter 122 extends outwardly from sleeve 84 and track 86in a direction toward guide catheter mechanism 26. In one embodiment,connecting portion 136 has sufficient length to allow for the guidecatheter hub to be connected to rotating luer 52 and have sufficientlength to bend into track 86. Connecting portion 136 extends outwardlyfrom sleeve 84 at angle between approximately 25 to 45 degrees and 30 inbut may be between 30 and 45 degrees and may be 30 degrees. Guideportion 82 guides guide catheter from support 80 into track 86. Guideportion 82 may include a curved surface to assist in the transition ofthe guide catheter into track 86.

Proximal end 128 guide catheter 122 is connected to rotating luerconnector 48. In one embodiment, proximal end 128 of guide catheter 122is connected to rotating luer connector 48 of hemostasis valve 34 priorto distal end 124 of catheter 122 being inserted into the patient orprior to central portion 132 being positioned within sleeve 84.Hemostasis valve 34 is secured to base 32 with a quick release mechanism138 such that driven gear 56 is engaged with drive gear 58. Driven gear56 located on external surface 52 of rotating luer connector 48 is movedin a direction toward drive gear 58 to engage driven gear 56 with drivegear 58. Quick release 138 is then closed to releasably capturehemostasis valve 34. In an engaged position proximal end 46 of secondleg 44 of hemostasis valve extends away from track 86 and having ahorizontal vector component. Stated another way in a preferredembodiment, second leg working plane defined by axis 50 of first leg 38and axis 70 of second leg 44 does not define a plane that isperpendicular to a horizontal plane defined by gravity or by ahorizontal plane defined generally by the top surface of the patient'sbed 22.

Guide Catheter mechanism 26 is moved linearly by linear actuator 116 toallow proper alignment of proximal end 126 of guide catheter 122 withguide catheter mechanism 26. Guide catheters are typically sold withvarying lengths and selected depending on the size of the patient.However, since the length of the guide catheter required varies frompatient to patient, it may be necessary to adjust the position of thehemostasis valve quick release for each patient. In one embodimenthemostasis valve quick release may be adjusted along an axis parallel totrack axis 106 relative to base 32. In another embodiment, base 32 maybe moved along an axis parallel to track axis 106 to properly positionhemostasis valve 34 so that guide catheter 122 is properly positionedrelative to the patient.

Linear adjustment of hemostasis valve along an axis parallel to trackaxis 106 may be done manually or may be controlled by user interface 18at work station 14 that is typically remote from bedside system 12. Workstation 14 communicates with bedside system through a wireless or wiredconnection. In this embodiment, an operator manipulates user interface18 such as a joy stick or touch screen to provide a control signal to alinear actuator motor to move base 32 relative to track 86.

Once guide catheter 32 is secured to hemostasis valve 34 and hemostasisvalve 34 is secured to base 34 with quick release 138 a guide wire 140and/or working catheter 142 is introduced into the proximal end 42 offirst leg 38. Proximal end 42 of first leg 38 includes a valve member162 such as a Tuohy Borst adapter. Tuohy Borst adapters are known in theart and operate to adjust the size of the opening in proximal end 42 offirst leg 38 of hemostasis valve 34 to minimize the risk that fluids mayexit the proximal end 42 of first leg 38. Other types of adapters knownin the art may also be used with hemostasis valve 34 to adjust the sizeof the opening in proximal end 42 of first let 38.

During a catheter procedure it may be necessary to reseat distal end 124of guide catheter 122 within the ostium of the patient. An operator mayrotate guide catheter 122 by providing a control signal to motor 60 torotate drive gear 58 in a clockwise or counterclockwise direction. As aresult driven gear 56 rotates causing rotation of rotating luerconnector 48 and rotation of guide catheter 122. In addition to arequirement to rotate guide catheter 122 it may also be necessary duringa catheter procedure to move guide catheter 122 along track axis 106 toproperly position distal end 124 of guide catheter 122. Work station mayalso include a user interface such as a joy stick, button, touch screenor other user interface to control a linear actuator to move guidecatheter mechanism 26 in a direction substantially parallel to trackaxis 106. Movement in a first direction in parallel to track axis willresult in movement of guide catheter 122 further into the patient andmovement of the linear translator in an opposing second direction willresult in movement of guide catheter 122 outwardly from the patient.

If an operator wishes to remove guide catheter 122, working catheter 142and/or guide wire 140 during a catheter procedure, the operator releasesquick release 138 and removes hemostasis valve 34 along with guidecatheter 122 and working catheter 142 and/or guide wire 140. Centralportion 132 of guide catheter 122

Working catheter 142 and guide wire 140 may be removed from theirrespective working catheter mechanism 28 and guide wire mechanism 30 asdescribed in U.S. Pat. No. 7,887,549. Once guide catheter 122, 140hemostasis valve 34, working catheter 142 and guide wire 140 are removedfrom guide catheter mechanism 26, working catheter mechanism 28 andguide wire mechanism 30 an operator may manipulate guide catheter 122,working catheter 142 and guide wire 140 manually.

Referring to FIG. 13 an alternative embodiment of a drive for rotationalluer connector includes a motor 144 rotating a first pulley 146 drivinga belt 148 such as a timing belt. Belt 148 is connected to the outersurface 150 of a pulley 152 about the outer surface 150 of a rotationalluer connector 156. First pulley 146 may include a plurality of teeththat mesh with ribs on belt 148 and the outer surface 150 of rotationalluer connector 154 also include a plurality of teeth that mesh with ribson belt 148. In this manner control of motor 144 allows for controlledrotation in a clockwise and counterclockwise of rotational luerconnector 156 thereby rotating guide catheter 122 attached thereto. Inone embodiment pulley 152 and bevel gear 56 are integrally formed withthe outer surface of rotating luer connector. However, it is alsocontemplated that a collet having an outer surface defining a pulley orbevel gear may be secured to the outer surface of rotating luerconnector.

Referring to FIG. 14, in another embodiment, a luer extension member 158may act to connect proximal end 128 of guide catheter 122 to rotatingluer connector 48. Luer extension member 158 may include an outersurface having a gear 160 or pulley member to be operatively connectedto the rotational drive motor 60 via drive gear 58. In this embodiment,the rotational drive motor is operatively coupled to the outer surfaceof luer extension member and not directly to the outer surface of therotating luer connector. This permits the use of presently availablecommercially available hemostasis valves. Additionally in a furtherembodiment a luer extension member may include a rotating portion suchthat the distal end of the hemostasis valve need not have a rotationalluer connector but rather include a non-rotational luer connector.Extension 158 includes a female luer connector on the distal end toremovably receive a male luer fitting on a guide catheter. Extension 158also includes a male luer connector on the proximal end that isremovably received within a female luer connector of a rotatingconnector on a Hemostasis valve. Note that in one embodiment, gear 160is a beveled gear with teeth facing the proximal end.

Referring to FIG. 15 in another embodiment, a hub of guide catheter 122may have gear formed therewith or attached thereto to connect to arotating luer of hemostasis valve 34. Referring to FIG. 16-FIG. 18 arelease 234 includes a lever 238 that releasably engages hemostasisvalve 34.

Referring to FIG. 19, an extension member 158 is interposed between aY-connector or hemostasis valve 34 and a guide catheter 22. Thisextension member 158 interacts with the drive gear 58, the guidecatheter 122 and the Y-connector or hemostasis valve 34 to impartrotation to the guide catheter 122 while isolating the valve 34 fromrotational motion such that the position of the second leg 44 of thevalve 34 does not change position when the guide catheter 122 isrotated. The bracket 190 interacts with the groove 182 in the extensionmember 158 to provide it support as it rotates and is itself secured toeither base 32 or wall 74. The valve 34 is supported by bracket 192 thatis itself secured to either base 32 or wall 74. The two brackets 190 and192 provide stability to the longitudinal axis 50 of the valve 34. Theproximate end 128 of the guide catheter 122 provides a luer interlockwith the extension member 158. Guide member 80 and track 86 providesupport for the guide catheter 122 as it extends in the distal directionaway from the extension member 158 and toward the patient bed 22 shownin FIG. 2. The extension member 158 is provided with a beveled gear face160 which can be rotated by the drive gear 58 to impart rotation to theguide catheter 122, although other means can be used to impart rotationto the extension member 158, such as that illustrated in FIG. 22. Thedrive gear 58 is in turn rotated by motor 60.

Referring to FIG. 20, the extension member 158 may be composed of aninner piece 170 and an outer piece 180. The inner piece 170 has a maleluer lock 172 that interacts with receptacle 129 on the guide catheter128 to provide a fluid tight connection. It also has a female luer lockthat forms a rotational fluid tight seal with protuberance 41 on thevalve 40. Piece 170 is frictionally captured by the bore of outer piece180 that has a collar 184 that helps to define the groove 182 thatinteracts with the bracket 190. Outer piece 180 also carries the beveledgear face 160. The frictional capture of inner piece 170 is such thatouter piece 180 can readily transfer rotational motion to it.Alternatively, inner piece 170 and outer piece 180 could be molded as asingle article.

Referring to FIG. 21, the composite structure of guide catheter 122,extension member 158 and valve 34 is shown along section line 21-21 ofFIG. 19. The second leg 44 of the valve 34 has a proximal end 46, adistal end 72 and a longitudinal axis 70. Inner piece 170 is nestedinside the bore of outer piece 180. Male luer lock 172 engages thereceptacle 129 at the proximal end 128 of the guide catheter 122 whilefemale luer lock 174 forms a fluid tight rotational seal with theprotuberance 41 on the distal end 40 of the valve 34. There is acontinuous fluid path from the proximate end 42 of the valve 34 to thebore of the guide catheter 122.

Referring to FIG. 22, an alternative extension member 159 can be used toimpart rotational motion to the guide catheter 122 without carrying gearteeth. The drive gear 58 drives gear 160 that frictionally engages theouter surface of the extension member 159 with an O-Ring 200. The gear160 could carry any means of frictional transfer to interact with thealternative extension member 159. The extension member 159 has a maleluer lock 174 that engages the valve 34 to form a rotational seal.

Further modifications and alternative embodiments of various aspects ofthe invention will be apparent to those skilled in the art in view ofthis description. Accordingly, this description is to be construed asillustrative only. The construction and arrangements, shown in thevarious exemplary embodiments, are illustrative only. Although only afew embodiments have been described in detail in this disclosure, manymodifications are possible (e.g., variations in sizes, dimensions,structures, shapes and proportions of the various elements, values ofparameters, mounting arrangements, use of materials, colors,orientations, etc.) without materially departing from the novelteachings and advantages of the subject matter described herein. Someelements shown as integrally formed may be constructed of multiple partsor elements, the position of elements may be reversed or otherwisevaried, and the nature or number of discrete elements or positions maybe altered or varied. The features described herein may be combined inany combination and such combinations are contemplated. The order orsequence of any process, logical algorithm, or method steps may bevaried or re-sequenced according to alternative embodiments. Othersubstitutions, modifications, changes and omissions may also be made inthe design, operating conditions and arrangement of the variousexemplary embodiments without departing from the scope of the presentinvention.

What is claimed is:
 1. An apparatus, comprising: a hemostasis valveincluding a valve body having a proximal port, a distal port and a lumenextending between the proximal port and the distal port, at least onevalve being located in the lumen to permit an interventional device tobe passed therethrough, a rotating connector rotatably connected to thedistal port configured to secure a catheter thereto, the rotatingconnector having a rotating linear bearing surface and a driven memberconfigured to be rotatably driven by a drive mechanism, the catheterrotatingly coupled with the rotating connector; the valve body having avalve body longitudinal axis extending through the proximal port anddistal port; and a base having a first linear bearing surface contactingthe rotating linear bearing surface prohibiting movement of the rotatingconnector in a direction parallel to the valve body longitudinal axis.2. The apparatus of claim 1, wherein the driven member is a hollowconnector having a lumen receiving a female connector removably coupledto the rotating connector which is a male connector, the femaleconnector extending from the catheter.
 3. The apparatus of claim 2,wherein the male connector is a male luer connector and the femaleconnector is a female luer connector.
 4. The apparatus of claim 1,wherein the driven member includes a gear, and the rotating linearbearing surface rotates with the driven member and is proximate to thedriven member.
 5. The apparatus of claim 4, wherein the gear is abeveled gear having a plurality of teeth facing toward the proximalport.
 6. The apparatus of claim 4, wherein the gear and the rotatingconnector are integrally formed as a single component.
 7. The apparatusof claim 4, wherein the gear is removably coupled to the rotatingconnector.
 8. The apparatus of claim 1, further including a bracketconfigured to receive a surface of the valve body.
 9. The apparatus ofclaim 1, wherein the at least one valve includes a resilient materialdefining an opening, the resilient material being configured to deformand form a seal around the interventional device that is extendingthrough the opening and through the lumen.
 10. The apparatus of claim 1,wherein the base includes a second linear bearing surface interactingwith a linear bearing surface on the hemostasis valve prohibitingmovement of the rotating connector in a distal direction parallel to thevalve body longitudinal axis.
 11. The apparatus of claim 10, wherein thefirst linear bearing surface is proximal to the second linear bearingsurface.
 12. An apparatus comprising: a hemostasis valve including avalve body with a first leg having a proximal port, a distal port and alumen extending between the proximal port and the distal port, at leastone valve being located in the lumen adjacent the proximal port topermit an interventional device to be passed therethrough, the valvebody including a second leg extending at an angle relative to the firstleg and in fluid communication with the first leg, a rotating connectorrotatably connected to the valve body proximate the distal port, therotating connector having a driven member and a rotating linear bearingsurface, the valve body having a valve body longitudinal axis extendingthrough the proximal port and distal port; a catheter, releasablycoupled to the rotating connector, the catheter having a catheterlongitudinal axis; a drive mechanism having a drive member removablyinterfacing with the driven member, and a motor operatively connected tothe drive member, the motor rotating the catheter about the catheterlongitudinal axis in a first direction and opposing second direction inresponse to rotation of the motor in a first direction about an axis ofthe motor and an opposing second direction about the axis of the motor,through rotation of the drive member, driven member and rotating lockconnector; and a base having a first linear bearing surface contactingthe rotating linear bearing surface prohibiting movement of the rotatingconnector in a direction parallel to the valve body longitudinal axis.13. The apparatus of claim 12, wherein the driven member includes agear, and the rotating linear bearing surface rotates with the drivenmember and is proximate to the driven member.
 14. The apparatus of claim13, wherein the gear is a beveled gear having a plurality of teethfacing toward the proximal port, the drive member including a gearhaving a plurality of teeth operatively engaged with the plurality ofteeth of the driven member.
 15. The apparatus of claim 12, wherein therotating lock connector is a rotating male luer lock connector.
 16. Theapparatus of claim 12, wherein rotation of the motor includes rotationof a motor shaft.
 17. The apparatus of claim 12, wherein the baseincludes a second linear bearing surface interacting with a linearbearing surface on the hemostasis valve prohibiting movement of therotating connector in a distal direction parallel to the valve bodylongitudinal axis.
 18. The apparatus of claim 17, wherein the firstlinear bearing surface is proximal to the second linear bearing surface.